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Plos One|May 8, 2014
Genome-wide association study of maternal and inherited loci for conotruncal heart defectsA J Agopian, Laura E Mitchell, Joseph Glessner, et al.Plos One|July 18, 2019
Gene-based genome-wide association studies and meta-analyses of conotruncal heart defectsAnshuman Sewda, A J Agopian, Elizabeth Goldmuntz, et al.Pediatric Clinics of North America|November 25, 2004
The genetic contribution to congenital heart diseaseElizabeth GoldmuntzBirth Defects Research. Part A, Clinical and Molecular Teratology|September 5, 2008
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndromeElizabeth Goldmuntz, Deborah A Driscoll, Beverly S Emanuel, et al.Plos One|June 10, 2020
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defectsAnshuman Sewda, A J Agopian, Elizabeth Goldmuntz, et al.Pediatric Cardiology|April 23, 2013
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive casesShabnam Peyvandi, Philip J Lupo, Jennifer Garbarini, et al.Biodata Mining|February 13, 2022
Gene-Interaction-Sensitive enrichment analysis in congenital heart diseaseAlexa A Woodward, Deanne M Taylor, Elizabeth Goldmuntz, et al.Human Molecular Genetics|August 21, 2014
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformationsLaura E Mitchell, A J Agopian, Angela Bhalla, et al.Methods in Molecular Medicine|August 26, 2006
The cardiovascular manifestations of Alagille syndrome and JAGI mutationsElizabeth Goldmuntz, Elizabeth Moore, Nancy B SpinnerPageof 30